This position is responsible for establishing and managing a global occupational and environmental toxicology program. The individual will be required to provide stewardship and support for Vertex's project portfolio. The individual will be part of the global environmental health and safety (EHS) team responsible for setting standards, developing culture and programs esta

P lay a critical role in setting up in house chargeback function , working cross functionally with 3 PL, Trade & Distribution, Accounting, and DTE, etc. to develop policies, efficient processes, system requirements, and department al SOPs . Partner with Government Pricing & Programs , Contract Operations , Payer Accounts and Legal, etc. to p rovide key insights during con

The Senior Director, Quality GLP, Biomarkers and Research has overall accountability for strategic leadership and oversight of the end to end quality assurance strategy for proactive, risk informed, and sustainable quality oversight and compliance with regulatory expectations across Vertex processes for clinical evidence generation and product vigilance Key Duties and Res

Vertex Pharmaceuticals Inc. has established a state of the art GMP manufacturing facility in Boston less than a mile from the Corporate Headquarters in the Seaport District. This GMP facility is a keystone to delivering our strategy of bringing transformative medicines to patients in need, from clinical development to commercialization. The Senior Specialist will be respo

The Trade and Distribution Data Analytics Manager will be responsible for supporting insights activities. The insights are used to track business performance and provide key data to inform business decisions. The Manager will typically partner with their manager on key projects and will be responsible for running market research or data analysis. This is a hybrid/on site

Define, plan and execute the full scope of assigned projects. Ability and willingness to perform project tasks at all levels to meet the project needs, from basic to complex, both independently and collaboratively Identify, analyze, prioritize, communicate and mitigate project risks Manage multiple projects simultaneously to successful outcomes Forecast, track and manage

The Principal Biostatistician will perform advanced scientific statistical analyses in support of the company's Global Medicines Development and Affairs area with some guidance and mentoring on new and complex issues. The incumbent will completed work in a resourceful, self sufficient manner and create alternative approaches to achieve desired results. The incumbent shoul

Vertex has established a new research site in Boston Seaport where research, development, and clinical manufacturing for cell and genetic therapies will be primarily based. Cell and genetic therapies represent two rapidly emerging therapeutic modalities with the potential to treat and even cure several of the diseases Vertex is focused on, including sickle cell disease, D

Provides leadership and oversight of DASH/Disease area Safety Team(s) (DST) conduct, for all products across the Vertex Portfolio, including pre FIH activities, key benefit risk assessment, and providing strategy for DSTs to meet goals and objectives. Coordinates and oversees the consistent and timely review of safety data for identification of new safety signals, in acco

Provides leadership and oversight of Safety Team(s) for products within assigned therapeutic area(s), including pre FIH activities, benefit risk assessment, and strategy for DSTs. Coordinates and oversees safety signals detection, in accordance with Vertex signal detection practices. Collaborates with Clinical Leaders to develop and implement appropriate Risk Management p

The GMP Quality Operations Director serves as a Quality leader in the areas of process validation, and equipment validation in oral solid dosage form. The Director is also responsible for managing multiple department activities with a high degree of independence while providing oversight of the development, implementation, and maintenance of relevant quality initiatives i

The Training Associate Director is responsible for supporting the oversight of all Training related activities within the Global Regulatory Affairs organization. This role will work to create, curate, and deliver top notch learning experiences including both technical and professional development for the team. The Training Associate Director will report directly to the Se

The Director, Modeling & Simulations (M&S) Pharmacometrics will be responsible forindependently determining, planning, and executing M&S analyses for an entire drug development program in close collaboration with cross functional colleagues within the R&D organization. In this role, it is expected that the incumbent will represent M&S with cross functional drug developmen

Lead and ensure successful development and implementation of the commercialization (midterm) and portfolio (long term) strategies including brand development, competitive strategy, go to market/launch, and lifecycle decisions for future launches. Executed in close partnership with the Regions, Market Access, Regulatory and Commercial Manufacturing. Develop strong partners

Build and manage a manufacturing engineering team for DSDP cells and combination products Act as primary technical and engineering manufacturing lead design reviews, documentation with focus on designing for manufacturability. Implement, propose and drive the implementation of Drug Product Device and manufacturing engineering controls by integrating Vertex QMS, production